| Literature DB >> 34570661 |
Viorel Simion1, Claire Loussouarn2, Yoan Laurent1, Loris Roncali2, David Gosset1, Flora Reverchon1, Audrey Rousseau2, Francisco Martin3, Patrick Midoux1, Chantal Pichon1, Emmanuel Garcion2, Patrick Baril1.
Abstract
A major unresolved challenge in miRNA biology is the capacity to monitor the spatiotemporal activity of miRNAs expressed in animal disease models. We recently reported that the miRNA-ON monitoring system called RILES (RNAi-inducible expression Luciferase system) implanted in lentivirus expression system (LentiRILES) offers unique opportunity to decipher the kinetics of miRNA activity in vitro, in relation with their intracellular trafficking in glioblastoma cells. In this study, we describe in detail the method for the production of LentiRILES stable cell lines and employed it in several applications in the field of miRNA biology and therapy. We show that LentiRILES is a robust, highly specific and sensitive miRNA sensor system that can be used in vitro as a single-cell miRNA monitoring method, cell-based screening platform for miRNA therapeutics and as a tool to analyse the structure-function relationship of the miRNA duplex. Furthermore, we report the kinetics of miRNA activity upon the intracranial delivery of miRNA mimics in an orthotopic animal model of glioblastoma. This information is exploited to evaluate the tumour suppressive function of miRNA-200c as locoregional therapeutic modality to treat glioblastoma. Our data provide evidence that LentiRILES is a robust system, well suited to resolve the activity of endogenous and exogenously expressed miRNAs from basic research to gene and cell therapy.Entities:
Keywords: RILES; RNA therapeutics; glioblastoma; miRNA; molecular imaging
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Year: 2021 PMID: 34570661 PMCID: PMC8682973 DOI: 10.1080/15476286.2021.1978202
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.766